EP0021476B1 - Liquid fabric softener containing a quaternary ammonium salt and method of conditioning fabrics - Google Patents
Liquid fabric softener containing a quaternary ammonium salt and method of conditioning fabrics Download PDFInfo
- Publication number
- EP0021476B1 EP0021476B1 EP80200499A EP80200499A EP0021476B1 EP 0021476 B1 EP0021476 B1 EP 0021476B1 EP 80200499 A EP80200499 A EP 80200499A EP 80200499 A EP80200499 A EP 80200499A EP 0021476 B1 EP0021476 B1 EP 0021476B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- composition
- carbon atoms
- fabric conditioning
- weight
- component
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 239000004744 fabric Substances 0.000 title claims description 60
- 230000003750 conditioning effect Effects 0.000 title claims description 42
- 239000007788 liquid Substances 0.000 title claims description 16
- 238000000034 method Methods 0.000 title claims description 10
- 239000002979 fabric softener Substances 0.000 title claims description 7
- 150000003242 quaternary ammonium salts Chemical class 0.000 title description 3
- 239000000203 mixture Substances 0.000 claims description 82
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 41
- 125000004432 carbon atom Chemical group C* 0.000 claims description 40
- 150000001412 amines Chemical class 0.000 claims description 33
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 26
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 25
- 239000003795 chemical substances by application Substances 0.000 claims description 22
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 18
- 125000000217 alkyl group Chemical group 0.000 claims description 17
- -1 fatty acid ester Chemical class 0.000 claims description 17
- 150000002148 esters Chemical class 0.000 claims description 16
- 125000002091 cationic group Chemical group 0.000 claims description 14
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 12
- 229930195729 fatty acid Natural products 0.000 claims description 12
- 239000000194 fatty acid Substances 0.000 claims description 12
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 9
- 239000003760 tallow Substances 0.000 claims description 9
- 150000004665 fatty acids Chemical class 0.000 claims description 8
- 150000005690 diesters Chemical class 0.000 claims description 7
- IQDGSYLLQPDQDV-UHFFFAOYSA-N dimethylazanium;chloride Chemical compound Cl.CNC IQDGSYLLQPDQDV-UHFFFAOYSA-N 0.000 claims description 6
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 claims description 6
- 150000001735 carboxylic acids Chemical class 0.000 claims description 4
- 150000002191 fatty alcohols Chemical class 0.000 claims description 4
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 4
- 150000001335 aliphatic alkanes Chemical class 0.000 claims description 3
- 238000001035 drying Methods 0.000 claims description 3
- 150000005691 triesters Chemical class 0.000 claims description 3
- 238000005406 washing Methods 0.000 claims description 3
- 239000000306 component Substances 0.000 claims description 2
- 235000011187 glycerol Nutrition 0.000 description 8
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 6
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 6
- 239000003381 stabilizer Substances 0.000 description 6
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 5
- 230000008014 freezing Effects 0.000 description 5
- 238000007710 freezing Methods 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 239000002304 perfume Substances 0.000 description 5
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000004902 Softening Agent Substances 0.000 description 3
- 238000013019 agitation Methods 0.000 description 3
- 239000004202 carbamide Substances 0.000 description 3
- 239000003086 colorant Substances 0.000 description 3
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 3
- 239000000499 gel Substances 0.000 description 3
- YQEMORVAKMFKLG-UHFFFAOYSA-N glycerine monostearate Natural products CCCCCCCCCCCCCCCCCC(=O)OC(CO)CO YQEMORVAKMFKLG-UHFFFAOYSA-N 0.000 description 3
- SVUQHVRAGMNPLW-UHFFFAOYSA-N glycerol monostearate Natural products CCCCCCCCCCCCCCCCC(=O)OCC(O)CO SVUQHVRAGMNPLW-UHFFFAOYSA-N 0.000 description 3
- 229920006395 saturated elastomer Chemical group 0.000 description 3
- MPNXSZJPSVBLHP-UHFFFAOYSA-N 2-chloro-n-phenylpyridine-3-carboxamide Chemical compound ClC1=NC=CC=C1C(=O)NC1=CC=CC=C1 MPNXSZJPSVBLHP-UHFFFAOYSA-N 0.000 description 2
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- 235000021357 Behenic acid Nutrition 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 2
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 2
- SRBFZHDQGSBBOR-IOVATXLUSA-N D-xylopyranose Chemical compound O[C@@H]1COC(O)[C@H](O)[C@H]1O SRBFZHDQGSBBOR-IOVATXLUSA-N 0.000 description 2
- OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- SZQVPFAWVOAHPI-UHFFFAOYSA-N [O-]P([O-])([O-])=O.CCC[NH2+]CCC.CCC[NH2+]CCC.CCC[NH2+]CCC Chemical compound [O-]P([O-])([O-])=O.CCC[NH2+]CCC.CCC[NH2+]CCC.CCC[NH2+]CCC SZQVPFAWVOAHPI-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- PYMYPHUHKUWMLA-UHFFFAOYSA-N arabinose Natural products OCC(O)C(O)C(O)C=O PYMYPHUHKUWMLA-UHFFFAOYSA-N 0.000 description 2
- 230000001580 bacterial effect Effects 0.000 description 2
- SRBFZHDQGSBBOR-UHFFFAOYSA-N beta-D-Pyranose-Lyxose Natural products OC1COC(O)C(O)C1O SRBFZHDQGSBBOR-UHFFFAOYSA-N 0.000 description 2
- 239000004665 cationic fabric softener Substances 0.000 description 2
- 239000002752 cationic softener Substances 0.000 description 2
- 239000003599 detergent Substances 0.000 description 2
- XJAKUIIGQJMOHE-UHFFFAOYSA-M dihexadecyl(dimethyl)azanium;acetate Chemical compound CC([O-])=O.CCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCC XJAKUIIGQJMOHE-UHFFFAOYSA-M 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 150000002334 glycols Chemical class 0.000 description 2
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- VKOBVWXKNCXXDE-UHFFFAOYSA-N icosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCC(O)=O VKOBVWXKNCXXDE-UHFFFAOYSA-N 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 235000020778 linoleic acid Nutrition 0.000 description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000000600 sorbitol Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- ZORQXIQZAOLNGE-UHFFFAOYSA-N 1,1-difluorocyclohexane Chemical compound FC1(F)CCCCC1 ZORQXIQZAOLNGE-UHFFFAOYSA-N 0.000 description 1
- ASJSAQIRZKANQN-CRCLSJGQSA-N 2-deoxy-D-ribose Chemical compound OC[C@@H](O)[C@@H](O)CC=O ASJSAQIRZKANQN-CRCLSJGQSA-N 0.000 description 1
- RFVNOJDQRGSOEL-UHFFFAOYSA-N 2-hydroxyethyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCO RFVNOJDQRGSOEL-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- LSWKXNPXIJXDHU-UHFFFAOYSA-N 4-oxo-4-tetradecoxybutanoic acid Chemical compound CCCCCCCCCCCCCCOC(=O)CCC(O)=O LSWKXNPXIJXDHU-UHFFFAOYSA-N 0.000 description 1
- XZIIFPSPUDAGJM-UHFFFAOYSA-N 6-chloro-2-n,2-n-diethylpyrimidine-2,4-diamine Chemical compound CCN(CC)C1=NC(N)=CC(Cl)=N1 XZIIFPSPUDAGJM-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- IBJSFCWILUNBRE-VMNXYWKNSA-N CCCCCC\C=C/CCCCCCCC(=O)OCCOC(=O)CCCCCCC\C=C/CCCCCC Chemical compound CCCCCC\C=C/CCCCCCCC(=O)OCCOC(=O)CCCCCCC\C=C/CCCCCC IBJSFCWILUNBRE-VMNXYWKNSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- HAIWUXASLYEWLM-UHFFFAOYSA-N D-manno-Heptulose Natural products OCC1OC(O)(CO)C(O)C(O)C1O HAIWUXASLYEWLM-UHFFFAOYSA-N 0.000 description 1
- WQZGKKKJIJFFOK-QTVWNMPRSA-N D-mannopyranose Chemical compound OC[C@H]1OC(O)[C@@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-QTVWNMPRSA-N 0.000 description 1
- HMFHBZSHGGEWLO-SOOFDHNKSA-N D-ribofuranose Chemical compound OC[C@H]1OC(O)[C@H](O)[C@@H]1O HMFHBZSHGGEWLO-SOOFDHNKSA-N 0.000 description 1
- 229930091371 Fructose Natural products 0.000 description 1
- 239000005715 Fructose Substances 0.000 description 1
- RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- OWYWGLHRNBIFJP-UHFFFAOYSA-N Ipazine Chemical compound CCN(CC)C1=NC(Cl)=NC(NC(C)C)=N1 OWYWGLHRNBIFJP-UHFFFAOYSA-N 0.000 description 1
- HSNZZMHEPUFJNZ-UHFFFAOYSA-N L-galacto-2-Heptulose Natural products OCC(O)C(O)C(O)C(O)C(=O)CO HSNZZMHEPUFJNZ-UHFFFAOYSA-N 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- PYMYPHUHKUWMLA-LMVFSUKVSA-N Ribose Natural products OC[C@@H](O)[C@@H](O)[C@@H](O)C=O PYMYPHUHKUWMLA-LMVFSUKVSA-N 0.000 description 1
- HAIWUXASLYEWLM-AZEWMMITSA-N Sedoheptulose Natural products OC[C@H]1[C@H](O)[C@H](O)[C@H](O)[C@@](O)(CO)O1 HAIWUXASLYEWLM-AZEWMMITSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- TVXBFESIOXBWNM-UHFFFAOYSA-N Xylitol Natural products OCCC(O)C(O)C(O)CCO TVXBFESIOXBWNM-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- HMFHBZSHGGEWLO-UHFFFAOYSA-N alpha-D-Furanose-Ribose Natural products OCC1OC(O)C(O)C1O HMFHBZSHGGEWLO-UHFFFAOYSA-N 0.000 description 1
- WQZGKKKJIJFFOK-PHYPRBDBSA-N alpha-D-galactose Chemical compound OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@H]1O WQZGKKKJIJFFOK-PHYPRBDBSA-N 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 239000002280 amphoteric surfactant Substances 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 150000001450 anions Chemical group 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- PYMYPHUHKUWMLA-WDCZJNDASA-N arabinose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)C=O PYMYPHUHKUWMLA-WDCZJNDASA-N 0.000 description 1
- IPTLKMXBROVJJF-UHFFFAOYSA-N azanium;methyl sulfate Chemical compound N.COS(O)(=O)=O IPTLKMXBROVJJF-UHFFFAOYSA-N 0.000 description 1
- 229940116226 behenic acid Drugs 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 230000001351 cycling effect Effects 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- VKKVMDHHSINGTJ-UHFFFAOYSA-M di(docosyl)-dimethylazanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCCCCCC VKKVMDHHSINGTJ-UHFFFAOYSA-M 0.000 description 1
- OCTAKUVKMMLTHX-UHFFFAOYSA-M di(icosyl)-dimethylazanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCCCC OCTAKUVKMMLTHX-UHFFFAOYSA-M 0.000 description 1
- HPDYVEVTJANPRA-UHFFFAOYSA-M diethyl(dihexadecyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+](CC)(CC)CCCCCCCCCCCCCCCC HPDYVEVTJANPRA-UHFFFAOYSA-M 0.000 description 1
- HDITUCONWLWUJR-UHFFFAOYSA-N diethylazanium;chloride Chemical compound [Cl-].CC[NH2+]CC HDITUCONWLWUJR-UHFFFAOYSA-N 0.000 description 1
- XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 1
- 229940075557 diethylene glycol monoethyl ether Drugs 0.000 description 1
- GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 description 1
- ZCPCLAPUXMZUCD-UHFFFAOYSA-M dihexadecyl(dimethyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCC ZCPCLAPUXMZUCD-UHFFFAOYSA-M 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- PGZPBNJYTNQMAX-UHFFFAOYSA-N dimethylazanium;methyl sulfate Chemical compound C[NH2+]C.COS([O-])(=O)=O PGZPBNJYTNQMAX-UHFFFAOYSA-N 0.000 description 1
- REZZEXDLIUJMMS-UHFFFAOYSA-M dimethyldioctadecylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCC REZZEXDLIUJMMS-UHFFFAOYSA-M 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 235000021588 free fatty acids Nutrition 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 229930182830 galactose Natural products 0.000 description 1
- 230000002070 germicidal effect Effects 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 125000005456 glyceride group Chemical group 0.000 description 1
- 150000002314 glycerols Chemical class 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical group C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 239000002563 ionic surfactant Substances 0.000 description 1
- 229940037626 isobutyl stearate Drugs 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 238000004900 laundering Methods 0.000 description 1
- OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 description 1
- CPXCDEMFNPKOEF-UHFFFAOYSA-N methyl 3-methylbenzoate Chemical compound COC(=O)C1=CC=CC(C)=C1 CPXCDEMFNPKOEF-UHFFFAOYSA-N 0.000 description 1
- WYTNTFGZBBTWNR-UHFFFAOYSA-M methyl sulfate;trimethyl(octadecyl)azanium Chemical compound COS([O-])(=O)=O.CCCCCCCCCCCCCCCCCC[N+](C)(C)C WYTNTFGZBBTWNR-UHFFFAOYSA-M 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- KTAFYYQZWVSKCK-UHFFFAOYSA-N n-methylmethanamine;nitric acid Chemical compound CNC.O[N+]([O-])=O KTAFYYQZWVSKCK-UHFFFAOYSA-N 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- NELAVKWPGRMFEQ-UHFFFAOYSA-N octane-1,4-diol Chemical compound CCCCC(O)CCCO NELAVKWPGRMFEQ-UHFFFAOYSA-N 0.000 description 1
- 235000021313 oleic acid Nutrition 0.000 description 1
- 150000002889 oleic acids Chemical class 0.000 description 1
- 239000003605 opacifier Substances 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000223 polyglycerol Polymers 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 150000003839 salts Chemical group 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- HSNZZMHEPUFJNZ-SHUUEZRQSA-N sedoheptulose Chemical compound OC[C@@H](O)[C@@H](O)[C@@H](O)[C@H](O)C(=O)CO HSNZZMHEPUFJNZ-SHUUEZRQSA-N 0.000 description 1
- 239000008234 soft water Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 229940035044 sorbitan monolaurate Drugs 0.000 description 1
- 239000001593 sorbitan monooleate Substances 0.000 description 1
- 235000011069 sorbitan monooleate Nutrition 0.000 description 1
- 229940035049 sorbitan monooleate Drugs 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- 238000010257 thawing Methods 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 239000004034 viscosity adjusting agent Substances 0.000 description 1
- 239000000811 xylitol Substances 0.000 description 1
- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 description 1
- 235000010447 xylitol Nutrition 0.000 description 1
- 229960002675 xylitol Drugs 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
- D06M13/46—Compounds containing quaternary nitrogen atoms
- D06M13/463—Compounds containing quaternary nitrogen atoms derived from monoamines
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/835—Mixtures of non-ionic with cationic compounds
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/001—Softening compositions
- C11D3/0015—Softening compositions liquid
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
- D06M13/46—Compounds containing quaternary nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/38—Cationic compounds
- C11D1/42—Amino alcohols or amino ethers
- C11D1/44—Ethers of polyoxyalkylenes with amino alcohols; Condensation products of epoxyalkanes with amines
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/38—Cationic compounds
- C11D1/62—Quaternary ammonium compounds
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/667—Neutral esters, e.g. sorbitan esters
Definitions
- This invention relates to compositions and methods for conditioning fabrics during the rinse cycle of home laundering operations. This is a widely used practice to impart to laundered fabrics a texture or handle that is smooth, pliable and fluffy to the touch (i.e. soft) and also to impart to the fabrics a reduced tendency to pick up and/or retain an electrostatic charge (i.e. static control), especially when the fabrics are dried in an automatic dryer.
- an electrostatic charge i.e. static control
- fabric conditioning compositions comprising major amounts of water, lesser amounts of fabric conditioning agents, and minor amount of optional ingredients such as perfumes, colorants, preservatives and stabilizers.
- Such compositions are aqueous suspensions or emulsions which can be conveniently added to the rinsing bath of home laundry operations.
- Liquid compositions based on non-cyclic quaternary ammonium cationic softeners are the historical basis of the household softener industry. They have traditionally suffered from inability to recover their fluid characteristics after freezing, which sometimes occurs during transportation or warehousing.
- Katsumi et al U.S. Pat. No. 3,850,818 issued Nov. 26, 1974 disclosed certain ethoxylated quaternary salts as fabric conditioning agents, admixed in specified proportions with conventional quaternaries and with one or more of the following additives: C'-3 alcohols, glycols, glycerol, sorbitol and urea.
- Katsumi's ethoxylated quaternaries have the structure where R, is long chain alkyl; R 2 is benzyl or an alkyl group having from 1 to 3 carbon atoms; the sum (m+n) is from 20 to 100; and X is Cl, Br or C 2 H 5 SO 4 .
- the Katsumi compositions were said to have good viscosity stability and freeze-thaw recovery.
- the protonated di-polyethoxy monoalkylamine and lower alcohol to be an effective stabilizing mixture in specific situations is, surprisingly, an effective stabilizer in ordinary softener compositions containing non-cyclic quaternary ammonium cationic softening agents.
- the stabilizer mixture of this invention comprises materials which are themselves chemically stable during prolonged periods of storage and warehousing, unlike those stabilizer mixtures of the prior art containing urea which introduce an inescapable risk of developing an odor problem caused by hydrolysis to ammonia and carbon dioxide under severe conditions of time, temperature and/or pH during storage. Thus a long felt need in the softener industry is satisfied.
- the present invention relates to fabric conditioning compositions in liquid form for use in home laundry operations.
- These compositions comprise the following essential components: (a) from 2% to 11%, preferably from 3% to 8%, of a non-cyclic quaternary ammonium cationic fabric conditioning agent; (b) from 0.1% to 1.3%, preferably from 0.3% to 1.0%, of protonated di-polyethoxy monoalkyl amine; (c) from 1% to 6%, preferably from 3% to 5%, of a lower alcohol as hereinafter defined; (d) from 1% to 5% by weight of the composition of a nonionic fabric conditioning agent which is a: i) C,o-CZ6 fatty acid ester of mono- or poly-hydroxy alcohols containing 1 to 12 carbon atoms; or an ii) ester of fatty alcohols having from 12 to 24 carbon atoms in the alkyl chain and mono- or poly-carboxylic acids having from 1 to 8 carbon atoms in the alkyl chain
- this invention provides a process of treating fabrics with the compositions defined above.
- compositions of the present invention contain, as component (a), cationic fabric conditioning agent.
- fabric conditioning is meant both fabric softening and fabric antistat effects.
- Fabric conditioning agents generally, are organic waxy materials having a melting/softening point between 25°C and 115°C, and are dispersible but not soluble in water.
- the amount of fabric conditioning agent in the compositions of this invention is from 2% to 11 %, preferably from 3% to 8%, by weight of the composition.
- the lower limits are amounts needed to contribute effective fabric conditioning performance when added to laundry rinse baths in the manner which is customary in home laundry practice.
- the upper limits are amounts beyond which physical instability problems arise in connection with storage of the liquid compositions. It will be appreciated that the conditions of storage greatly affect stability, and the formulator of fabric conditioning compositions with ordinary skill in the art can readily determine compositions having sufficient physical stability for his particular climate and warehouse storage conditions.
- physical stability herein is meant the ability of a composition to maintain a homogeneous condition and approximately a constant viscosity for long periods of storage. In commercial practice, such storage may be at various temperatures that hold approximately constant both above and below the normal ambient, and also at various cycling temperatures including those below the freezing point.
- the fabric conditioning agent of this invention is a quaternary ammonium salt having the formula: wherein R, is hydrogen or an aliphatic group having from 1 to 22 carbon atoms; R 2 is an aliphatic group having from 10 to 22 carbon atoms; R 3 and R 4 are each alkyl groups having from 1 to 3 carbon atoms; and X is an anion selected from the halogen, acetate, phosphate, nitrate and methyl sulfate radicals.
- non-cyclic quaternary ammonium salts include tallow trimethyl ammonium chloride; ditallow dimethyl ammonium chloride; ditallow dimethy ammonium methyl sulfate; dihexadecyl dimethyl ammonium chloride; di(hydrogenated tallow) dimethyl ammonium chloride; dioctadecyl dimethyl ammonium chloride; dieicosyl dimethyl ammonium chloride; didocosyl dimethyl ammonium chloride; di(hydrogenated tallow) dimethyl ammonium methyl sulfate; dihexadecyl diethyl ammonium chloride; dihexadecyl dimethyl ammonium acetate, ditallow dipropyl ammonium phosphate, ditallow dimethyl ammonium nitrate, and di(coconut-alkyl) dimethyl ammonium chloride.
- An especially preferred quaternary ammonium fabric conditioning agent is ditallow dimethyl ammonium chloride that is commercially available from General Mills, Inc. under the tradename ALI ⁇ UAT-2HT® and from the Sherex Chemical Company, Inc. as ADOGEN 448@.
- Component (b) of this invention is a protonated di-polyethoxy monoalkyl amine of formula:
- R 9 is an alkyl group, saturated or unsaturated, preferably having from 10 to 20 carbon atoms, most preferably from 14 to 18 carbon atoms; and the sum (m+n) is preferably from 10 to 40, most preferably from 16 to 30, where m and n are each integers greater than 1.
- the amount of protonated di-polyethoxy monoalkyl amine (hereinafter sometimes referred to simply as 'amine') in the compositions of this invention is from 0.1 % to 1.3%, preferably from 0.3% to 1.0%, by weight of the composition.
- 'amine' protonated di-polyethoxy monoalkyl amine
- it provides physical stability to the composition, especially at elevated temperatures and in multiple freeze-thaw cycles.
- a greater amount of amine confers stability under more severe conditions of storage.
- Incorporation of the protonated amine is ordinarily accomplished by adding the corresponding free, unprotonated amine to the remainder of the composition which, as compared to the amine, is acidic in nature. Depending upon the pH of the final composition, minor amounts of unprotonated amine may remain.
- Di-polyethoxy monoalkyl amines are made by ethoxylating monoalkyl amines in a conventional manner.
- An especially preferred amine has an alkyl group derived from unhardened tallow and the sum (m+n) is equal to 23.
- This amine is commercially available from Daiichi Kogyo Seiyaku Co., Ltd. of Japan under the tradename AMILADIN-D@.
- Another preferred amine made from unhardened tallow and having (m+n) equal to 20 is VARONIC T220® sold commercially by the Sherex Chemical Company, Inc.
- Certain ETHOMEENS® sold commercially by the Armak Company are also di-polyethoxy monoalkyl amines within the definition of component (b).
- Component (c) of this invention comprises from 196 to 6%, preferably from 3% to 5%, by weight of the composition of a lower alcohol.
- lower alcohol herein is meant monohydroxyalkanes having from 1 to 6 carbon atoms in either straight or branched chain configuration, for example ethanol, isopropanol, and n-hexanol; dihydroxyalkanes having from 2 to 8 carbon atoms, for example propylene glycol and 1,4-dihydroxy octane; and glycol ethers having from 4 to 16 carbon atoms, for example diethylene glycol monoethyl ether and polyethylene glycol having an average molecular weight of 370. Ethylene glycol is a preferred lower alcohol.
- compositions herein further comprise from 1% to 5% of a nonionic fabric conditioning agent which is a: i) C 10 ⁇ C 26 fatty acid ester of mono- or poly-hydroxy alcohols containing 1 to 12 carbon atoms; or an ii) ester of fatty alcohols having from 12 to 24 carbon atoms in the alkyl chain and mono-or poly-carboxylic acids having from 1 to 8 carbon atoms in the alkyl chain; whereby the total number of carbon atoms in the ester is equal to or greater than 16.
- a nonionic fabric conditioning agent which is a: i) C 10 ⁇ C 26 fatty acid ester of mono- or poly-hydroxy alcohols containing 1 to 12 carbon atoms; or an ii) ester of fatty alcohols having from 12 to 24 carbon atoms in the alkyl chain and mono-or poly-carboxylic acids having from 1 to 8 carbon atoms in the alkyl chain; whereby the total number of carbon atoms in the ester is equal
- the total amount of cationic plus nonionic fabric conditioning agents is no more than 1196.
- nonionic fabric conditioning agents are substantially water-insoluble.
- One preferred group thereof comprises C, o -C Z6 fatty acid esters of mono- or poly-hydroxy alcohols containing 1 to 12 carbon atoms. It is especially preferred that the alcohol have 1 to 8 carbon atoms, and it is preferred that the fatty acid ester has at least 1, more preferably at least 2, free (i.e. unesterified) hydroxyl groups.
- the mono- or poly-hydric alcohol portion of the ester can be represented by methanol, isobutanol, 2-ethylhexanol, isopropanol, ethylene glycol and polyethylene glycol with a maximum of 5 ethylene glycol units, glycerol, diglycerol, polyglycerol, xylitol, erithritol, pentaerythritol, sorbitol or sorbitan, sugars such as glucose, fructose, galactose, mannose, xylose, arabinose, ribose, 2-deoxyribose, sedoheptulose and sucrose.
- Ethylene glycol, glycerol and sorbitan esters are particularly preferred, especially the monoesters of glycerol.
- the fatty acid portion of the ester normally comprises a fatty acid having from 12 to 22 carbon atoms, typical examples being lauric acid, myristic acid, palmitic acid, stearic acid, arachidic acid and behenic acid, oleic and linoleic acid and some unsaturated higher fatty acids.
- the glycerol esters are very highly preferred. These are the mono-, di- or tri-esters of glycerol and fatty acids of the class described above. Commercial glycerol mono-stearate, which may contain a proportion of di- and tri-stearate, is suitable. Also useful are mixtures of saturated and unsaturated esters of glycerol derived from mixed saturated and unsaturated fatty acids.
- sorbitan esters Another very suitable group of nonionic softening agents is the sorbitan esters, and they are described in Murphy et al, U.S. Patent 4,085,052.
- Sorbitan mono- and di-esters of lauric, myristic, palmitic, stearic, arachidic or behenic, oleic or linoleic acids and unsaturated higher fatty acids are particularly useful as softening agents and can also provide antistatic benefits.
- Sorbitan esters are commercially available for instance under the Trade Name Span@.
- esters are constituted by esters of fatty alcohols having from 12 to 24 carbon atoms in the alkyl chain, and mono- or poly-carboxylic acids having from 1 to 8 carbon atoms in the alkyl chain, the total number of carbon atoms in the ester being at least 16.
- N nonionic fabric conditioning agents
- A protonated di-polyethoxymonoalkyl amine
- G ethylene glycol
- phase stability phenomena can be explained in general terms as follows.
- the dispersed particles are droplets of a phase comprising cationic and a high proportion of water.
- water is crystallized out of the droplets and, upon thawing, the droplets have a higher concentration of cationic than before: these droplets tend to coalesce causing increased viscosity and a tendency to gel.
- Protonated di-polyethoxy monoalkyl amine which is cationic in nature, is believed to penetrate the interior of the neat phase structure of the cationic fabric conditioner and, upon freezing, hold water within the droplets by hydrogen bonding to its polyethoxylate groups rather than allow the water to crystallize out as before.
- Lower alcohol is believed to inhibit water crystallization under practical storage conditions by a different but cooperative mechanism, viz. depression of the freezing point.
- a nonionic fabric conditioning agent When a nonionic fabric conditioning agent is added to a system already containing cationic conditioner, it too penetrates the interior of the near phase structure. Here it interferes with the action of the amine as described above, and greater amounts of amine are required to obtain its beneficial results.
- the preferred minimum amount of amine is no longer 0.2%, but as expressed in the first of the foregoing equations is greater than that figure by an amount which is proportional to the nonionic usage.
- Preferred fabric conditioning compositions of this invention comprise component (a) in a level from 3% to 8%, and component (b) in a level from 0.3% to 1.0% by weight of the composition of protonated di-polyethoxy monoalkylamine having the structural formula where R 9 is an alkyl group having from 10 to 20 carbon atoms and where (m+n) is from 10 to 40; and wherein component (c) is from 3% to 5% by weight of the composition and is selected from monohydroxyalkanes having from 1 to 6 carbon atoms, dihydroxy alkanes having from 2 to 8 carbon atoms, and glycol ethers having from 4 to 16 carbon atoms.
- component (a) is ditallow dimethyl ammonium chloride
- component (b) is protonated di-polyethoxy monoalkyl amine wherein Rg is an alkyl group derived from tallow and (m+n) is from 20 to 23
- component (c) is ethylene glycol, propylene glycol or ethanol
- component (d) is selected from mono-, di- and tri-esters of glycerol; mono- and di-esters of ethylene glycol; and esters of isobutanol; and wherein the number of carbon atoms in the fatty acid esterifying groups is from 12 to 18.
- the balance of the compositions of this invention is chiefly comprised of component (e), water.
- component (e) is the medium in which the essential components and the optional components, are dissolved, suspended or dispersed. Since minerals or other impurities in the water can react with certain of the other essential or optional composition components, it may be preferable to utilize deionized or soft water in the compositions herein.
- Optional components for use in liquid fabric conditioning compositions of this invention generally comprise from 0.1% to 10% by weight of the composition.
- Such optional components include but are not limited to, colorants, perfumes, bacterial inhibitors, optical brighteners, opacifiers, viscosity modifiers, fabric conditioning agents in solid form such as clay, fabric absorbency boosters, emulsifiers, stabilizers, shrinkage controllers, spotting agents, germicides, fungicides and anti-corrosion agents.
- the pH of the compositions of this invention is not critical, and may be anywhere in the normal range for cationic containing fabric softening compositions.
- the natural pH of the mixed components is ordinarily satisfactory; if adjustment is desired for any reason, trace quantities of organic or inorganic acids or bases can be used.
- a preferred pH range is 3.5 to 8.0; especially preferred is 4.5 to 6.5.
- the liquid fabric conditioning compositions of the present invention can be prepared by conventional methods. Homogenizing is not necessary. A convenient and satisfactory method is to prepare a premix of softeners in water at about 150°F (65.5°C) which is then added to a hot aqueous solution of the other ingredients. Temperature-sensitive optional components can be added after the fabric conditioning composition is cooled to room temperature or thereabouts.
- the liquid fabric conditioning compositions of this invention are used by adding to the rinse cycle of conventional home laundry operations.
- rinse water has a temperature of from about 5°C to about 60°C.
- concentration of the fabric conditioners of this invention, cationic plus nonionic is generally from about 2 ppm to about 200 ppm, preferably from about 10 ppm to about 100 ppm, by weight of the aqueous rinsing bath.
- the present invention in its fabric conditioning method aspect comprises (a) washing fabrics in a conventional washing machine with a detergent composition; (b) rinsing the fabrics; (c) adding during the rinsing stage of the operation the above-described amounts of cationic and nonionic fabric conditioner in an aqueous liquid composition containing specified amounts of protonated di-polyethoxymonoalkyl amine and lower alcohol as hereinbefore defined; and (d) drying the fabrics.
- the detergent composition normally contains an anionic, nonionic, amphoteric or ampholytic surfactant or a mixture thereof, and frequently contains in addition an organic or inorganic builder.
- the fabric conditioning composition is preferably added to the final rinse. Fabric drying can take place either in the open air or in an automatic dryer.
- Example 1 was prepared by the following process:
- the ⁇ complete composition was prepared as follows: 86.59 parts of city water [5-6 grains hardness/3.785 1) was metered into the mix tank and heated to 65°C. Then 0.0167 parts of 30% hydrogen peroxide solution was added, with agitation, followed by the addition of 1.67 parts of commercial di-polyethoxy monoalkyl amine (AMILADIN-D, 30% active, room temperature). After 1-2 minutes agitation to ensure thorough mixing, the heated softener premix prepared as described hereinbefore was added. Then 4.0 parts ethylene glycol, 0.17 parts perfume and 0.167 parts of Silicone (Dow-Corning's DC-436) were added, following which the entire composition was cooled from 65°C to 32°C with continued agitation. The pH was adjusted with dilute hydrochloric acid to 4.5. Batch size was 2000 grams.
- glycol monostearate of Example 1 was prepared by esterifying hardened soybean oil with glycerine. It contained 1.4% free fatty acid, and the remainder glycerides: 37% mono, 44% di, and 19% tri. The fatty acid chains were 10.2% palmitic, 88.8% stearic and 1.0% oleic, with traces of myristic and linoleic. Iodine value was 2.0.
- Example No. 1 was tested for fabric softening on cotton terry cloths and T-shirts and polyester and acrylic swatches, and was tested for antistatic effects on the foregoing synthetic fibers. It was found to be excellent in all these respects in comparison with commercially marketed products.
- Example 1 was repeated, except acid was not added to the final product and it remained at its natural pH of 5.6. Physical stability and softening performance were good; comparable in all respects to that of the product of Example 1.
- Example 2 was repeated except VARONIC T-220 was used instead of AMILADIN-D, and the batch size was increased to 400 pounds. Physical stability and softening performance were good in all respects.
- Example 1 was repeated with the variations in composition shown below: All of the above compositions also contained 0.001% Polar Blue, 0.005% hydrogen peroxide, 0.17% perfume and, except for composition 5, 0.10% DC-436 silicone. In these examples and those which follow, the glycerol monostearate was the same as specified in Example 1. In all examples, the balance of the composition is water.
- Example 1 was repeated with the variations in composition shown below. These are given for comparison purposes only, and are not examples of the instant invention because they do not contain both di-polyethoxy monoalkylamine and a lower alcohol.
- compositions of Examples 9-12 are within the scope of this invention; have good storage stability in relation to both elevated temperatures and freeze-thaw cycles; and have good fabric softening and antistat performance. Notes to Examples 9-12
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Textile Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Description
- This invention relates to compositions and methods for conditioning fabrics during the rinse cycle of home laundering operations. This is a widely used practice to impart to laundered fabrics a texture or handle that is smooth, pliable and fluffy to the touch (i.e. soft) and also to impart to the fabrics a reduced tendency to pick up and/or retain an electrostatic charge (i.e. static control), especially when the fabrics are dried in an automatic dryer.
- It has become commonplace today for homemakers to use fabric conditioning compositions comprising major amounts of water, lesser amounts of fabric conditioning agents, and minor amount of optional ingredients such as perfumes, colorants, preservatives and stabilizers. Such compositions are aqueous suspensions or emulsions which can be conveniently added to the rinsing bath of home laundry operations.
- Liquid compositions based on non-cyclic quaternary ammonium cationic softeners are the historical basis of the household softener industry. They have traditionally suffered from inability to recover their fluid characteristics after freezing, which sometimes occurs during transportation or warehousing.
- A number of prior art compositions, both as disclosed in the literature and as sold commercially, contain minor amounts of solvents to improve stability and/or control viscosity. For example, U.S. Pat. Nos. 3,954,634 granted on May 4, 1976 to Monson et al and 3,729,416 granted on Apr. 24, 1973 to Bruning et al, the latter mentioning alkanols, alkanediols, alkoxyalkane diols, and alkanones.
- Katsumi et al, U.S. Pat. No. 3,850,818 issued Nov. 26, 1974 disclosed certain ethoxylated quaternary salts as fabric conditioning agents, admixed in specified proportions with conventional quaternaries and with one or more of the following additives: C'-3 alcohols, glycols, glycerol, sorbitol and urea. Katsumi's ethoxylated quaternaries have the structure
- Davis disclosed in U.S. Patent 4,076,632 issued February 28, 1978 a physically stable liquid fabric softening composition comprising cationic fabric softener, protonated di-polyethoxy monoalkyl amine, urea, and water. Among the '632 cationics were quaternary ammonium salts, quaternary imidazolinium salts, and mixtures thereof. Solvents such as alcohols, glycols and glycol ethers were used optionally.
- It has now been found that the protonated di-polyethoxy monoalkylamine and lower alcohol to be an effective stabilizing mixture in specific situations is, surprisingly, an effective stabilizer in ordinary softener compositions containing non-cyclic quaternary ammonium cationic softening agents. The stabilizer mixture of this invention comprises materials which are themselves chemically stable during prolonged periods of storage and warehousing, unlike those stabilizer mixtures of the prior art containing urea which introduce an inescapable risk of developing an odor problem caused by hydrolysis to ammonia and carbon dioxide under severe conditions of time, temperature and/or pH during storage. Thus a long felt need in the softener industry is satisfied.
- In recent years, economic advantages have been shown for the use of various nonionic materials as fabric softeners when used in conjunction with cationic fabric softeners. Typical disclosures are Murphy et al, U.S. Patent 4,085,052 issued April 18, 1978; and Barford et al, U.S. Patent 4,128,484 issued Dec. 5, 1978. The amine/lower alcohol mixtures of the present invention have been found to impart physical stability also to mixed nonionic/cationic softening compositions.
- The present invention relates to fabric conditioning compositions in liquid form for use in home laundry operations. These compositions comprise the following essential components: (a) from 2% to 11%, preferably from 3% to 8%, of a non-cyclic quaternary ammonium cationic fabric conditioning agent; (b) from 0.1% to 1.3%, preferably from 0.3% to 1.0%, of protonated di-polyethoxy monoalkyl amine; (c) from 1% to 6%, preferably from 3% to 5%, of a lower alcohol as hereinafter defined; (d) from 1% to 5% by weight of the composition of a nonionic fabric conditioning agent which is a: i) C,o-CZ6 fatty acid ester of mono- or poly-hydroxy alcohols containing 1 to 12 carbon atoms; or an ii) ester of fatty alcohols having from 12 to 24 carbon atoms in the alkyl chain and mono- or poly-carboxylic acids having from 1 to 8 carbon atoms in the alkyl chain; whereby the total number of carbon atoms in the ester is equal to or greater than 16; wherein the total amount of cationic plus nonionic fabric conditioning agents is no more than 11 %, and (e) water. Minor amounts of other materials often used in liquid fabric conditioners can also be present, such as colorants, perfumes, bacterial inhibitors, and optical brighteners. In the foregoing recitation, all percentages are by weight based on the complete fabric conditioning composition.
- In its method aspect, this invention provides a process of treating fabrics with the compositions defined above.
- The compositions of the present invention contain, as component (a), cationic fabric conditioning agent. By fabric conditioning is meant both fabric softening and fabric antistat effects. Fabric conditioning agents, generally, are organic waxy materials having a melting/softening point between 25°C and 115°C, and are dispersible but not soluble in water.
- The amount of fabric conditioning agent in the compositions of this invention is from 2% to 11 %, preferably from 3% to 8%, by weight of the composition. The lower limits are amounts needed to contribute effective fabric conditioning performance when added to laundry rinse baths in the manner which is customary in home laundry practice. The upper limits are amounts beyond which physical instability problems arise in connection with storage of the liquid compositions. It will be appreciated that the conditions of storage greatly affect stability, and the formulator of fabric conditioning compositions with ordinary skill in the art can readily determine compositions having sufficient physical stability for his particular climate and warehouse storage conditions. By physical stability herein is meant the ability of a composition to maintain a homogeneous condition and approximately a constant viscosity for long periods of storage. In commercial practice, such storage may be at various temperatures that hold approximately constant both above and below the normal ambient, and also at various cycling temperatures including those below the freezing point.
- The fabric conditioning agent of this invention is a quaternary ammonium salt having the formula:
- Representative examples of non-cyclic quaternary ammonium salts include tallow trimethyl ammonium chloride; ditallow dimethyl ammonium chloride; ditallow dimethy ammonium methyl sulfate; dihexadecyl dimethyl ammonium chloride; di(hydrogenated tallow) dimethyl ammonium chloride; dioctadecyl dimethyl ammonium chloride; dieicosyl dimethyl ammonium chloride; didocosyl dimethyl ammonium chloride; di(hydrogenated tallow) dimethyl ammonium methyl sulfate; dihexadecyl diethyl ammonium chloride; dihexadecyl dimethyl ammonium acetate, ditallow dipropyl ammonium phosphate, ditallow dimethyl ammonium nitrate, and di(coconut-alkyl) dimethyl ammonium chloride.
- An especially preferred quaternary ammonium fabric conditioning agent is ditallow dimethyl ammonium chloride that is commercially available from General Mills, Inc. under the tradename ALIΩUAT-2HT® and from the Sherex Chemical Company, Inc. as ADOGEN 448@.
- Component (b) of this invention is a protonated di-polyethoxy monoalkyl amine of formula:
- The amount of protonated di-polyethoxy monoalkyl amine (hereinafter sometimes referred to simply as 'amine') in the compositions of this invention is from 0.1 % to 1.3%, preferably from 0.3% to 1.0%, by weight of the composition. In conjunction with the lower alcohol hereinbelow described, it provides physical stability to the composition, especially at elevated temperatures and in multiple freeze-thaw cycles. In general, within the limits herein, a greater amount of amine confers stability under more severe conditions of storage. Incorporation of the protonated amine is ordinarily accomplished by adding the corresponding free, unprotonated amine to the remainder of the composition which, as compared to the amine, is acidic in nature. Depending upon the pH of the final composition, minor amounts of unprotonated amine may remain.
- Di-polyethoxy monoalkyl amines are made by ethoxylating monoalkyl amines in a conventional manner. An especially preferred amine has an alkyl group derived from unhardened tallow and the sum (m+n) is equal to 23. This amine is commercially available from Daiichi Kogyo Seiyaku Co., Ltd. of Japan under the tradename AMILADIN-D@. Another preferred amine made from unhardened tallow and having (m+n) equal to 20 is VARONIC T220® sold commercially by the Sherex Chemical Company, Inc. Certain ETHOMEENS® sold commercially by the Armak Company are also di-polyethoxy monoalkyl amines within the definition of component (b).
- Component (c) of this invention comprises from 196 to 6%, preferably from 3% to 5%, by weight of the composition of a lower alcohol. By lower alcohol herein is meant monohydroxyalkanes having from 1 to 6 carbon atoms in either straight or branched chain configuration, for example ethanol, isopropanol, and n-hexanol; dihydroxyalkanes having from 2 to 8 carbon atoms, for example propylene glycol and 1,4-dihydroxy octane; and glycol ethers having from 4 to 16 carbon atoms, for example diethylene glycol monoethyl ether and polyethylene glycol having an average molecular weight of 370. Ethylene glycol is a preferred lower alcohol.
- The compositions herein further comprise from 1% to 5% of a nonionic fabric conditioning agent which is a: i) C10―C26 fatty acid ester of mono- or poly-hydroxy alcohols containing 1 to 12 carbon atoms; or an ii) ester of fatty alcohols having from 12 to 24 carbon atoms in the alkyl chain and mono-or poly-carboxylic acids having from 1 to 8 carbon atoms in the alkyl chain; whereby the total number of carbon atoms in the ester is equal to or greater than 16.
- The total amount of cationic plus nonionic fabric conditioning agents is no more than 1196.
- These nonionic fabric conditioning agents are substantially water-insoluble. One preferred group thereof comprises C,o-CZ6 fatty acid esters of mono- or poly-hydroxy alcohols containing 1 to 12 carbon atoms. It is especially preferred that the alcohol have 1 to 8 carbon atoms, and it is preferred that the fatty acid ester has at least 1, more preferably at least 2, free (i.e. unesterified) hydroxyl groups.
- The mono- or poly-hydric alcohol portion of the ester can be represented by methanol, isobutanol, 2-ethylhexanol, isopropanol, ethylene glycol and polyethylene glycol with a maximum of 5 ethylene glycol units, glycerol, diglycerol, polyglycerol, xylitol, erithritol, pentaerythritol, sorbitol or sorbitan, sugars such as glucose, fructose, galactose, mannose, xylose, arabinose, ribose, 2-deoxyribose, sedoheptulose and sucrose. Ethylene glycol, glycerol and sorbitan esters are particularly preferred, especially the monoesters of glycerol.
- The fatty acid portion of the ester normally comprises a fatty acid having from 12 to 22 carbon atoms, typical examples being lauric acid, myristic acid, palmitic acid, stearic acid, arachidic acid and behenic acid, oleic and linoleic acid and some unsaturated higher fatty acids.
- The glycerol esters are very highly preferred. These are the mono-, di- or tri-esters of glycerol and fatty acids of the class described above. Commercial glycerol mono-stearate, which may contain a proportion of di- and tri-stearate, is suitable. Also useful are mixtures of saturated and unsaturated esters of glycerol derived from mixed saturated and unsaturated fatty acids.
- Another very suitable group of nonionic softening agents is the sorbitan esters, and they are described in Murphy et al, U.S. Patent 4,085,052. Sorbitan mono- and di-esters of lauric, myristic, palmitic, stearic, arachidic or behenic, oleic or linoleic acids and unsaturated higher fatty acids are particularly useful as softening agents and can also provide antistatic benefits. Sorbitan esters are commercially available for instance under the Trade Name Span@. For the purpose of the present invention, it is preferred that a significant amount of di- and tri-sorbitan esters are present in the ester mixture. Ester mixtures having from 20%―50% monoester, 25%―50% di-ester and 10%―35% of tri- and tetra-esters are preferred.
- Another group of suitable esters is constituted by esters of fatty alcohols having from 12 to 24 carbon atoms in the alkyl chain, and mono- or poly-carboxylic acids having from 1 to 8 carbon atoms in the alkyl chain, the total number of carbon atoms in the ester being at least 16.
-
- The use of these relationships can be illustrated as follows. Assume that for performance reasons a formulator wishes to use, as softening ingredients 4% stearyl trimethyl ammonium methyl sulfate plus 3% sorbitan monooleate; and as stabilizing agents, AMILADIN-D amine plus ethylene glycol. From the first of the fore-going equations, the preferred usage of amine is at least [0.2+3/15]=0.4%. Now assume that the formulator chooses to use 0.5%, an amount well within the preferred range. Then the preferred usage of ethylene glycol is at least [4.5-2(0.5)]=3.5%. Selection of 4% usage by the formulator would be appropriate.
- The foregoing preferred limitations are in addition to those hereinbefore set forth for the amounts of amine and lower alcohol within the scope of this invention.
- Without wishing to be bound by theory, it is believed that phase stability phenomena can be explained in general terms as follows. In an ordinary emulsion system containing principally cationic softener and water, the dispersed particles are droplets of a phase comprising cationic and a high proportion of water. Upon freezing, water is crystallized out of the droplets and, upon thawing, the droplets have a higher concentration of cationic than before: these droplets tend to coalesce causing increased viscosity and a tendency to gel. Protonated di-polyethoxy monoalkyl amine, which is cationic in nature, is believed to penetrate the interior of the neat phase structure of the cationic fabric conditioner and, upon freezing, hold water within the droplets by hydrogen bonding to its polyethoxylate groups rather than allow the water to crystallize out as before. Lower alcohol is believed to inhibit water crystallization under practical storage conditions by a different but cooperative mechanism, viz. depression of the freezing point.
- When a nonionic fabric conditioning agent is added to a system already containing cationic conditioner, it too penetrates the interior of the near phase structure. Here it interferes with the action of the amine as described above, and greater amounts of amine are required to obtain its beneficial results. The preferred minimum amount of amine is no longer 0.2%, but as expressed in the first of the foregoing equations is greater than that figure by an amount which is proportional to the nonionic usage.
- Preferred fabric conditioning compositions of this invention comprise component (a) in a level from 3% to 8%, and component (b) in a level from 0.3% to 1.0% by weight of the composition of protonated di-polyethoxy monoalkylamine having the structural formula
- Preferred individual ingredients are as follows: component (a) is ditallow dimethyl ammonium chloride; component (b) is protonated di-polyethoxy monoalkyl amine wherein Rg is an alkyl group derived from tallow and (m+n) is from 20 to 23; component (c) is ethylene glycol, propylene glycol or ethanol, and component (d) is selected from mono-, di- and tri-esters of glycerol; mono- and di-esters of ethylene glycol; and esters of isobutanol; and wherein the number of carbon atoms in the fatty acid esterifying groups is from 12 to 18.
- In addition to components (a), (b), (c) and (d) as hereinbefore defined, the balance of the compositions of this invention is chiefly comprised of component (e), water. Water is the medium in which the essential components and the optional components, are dissolved, suspended or dispersed. Since minerals or other impurities in the water can react with certain of the other essential or optional composition components, it may be preferable to utilize deionized or soft water in the compositions herein.
- In addition to the essential components of this invention described hereinbefore, other components are optional. Optional components for use in liquid fabric conditioning compositions of this invention generally comprise from 0.1% to 10% by weight of the composition. Such optional components include but are not limited to, colorants, perfumes, bacterial inhibitors, optical brighteners, opacifiers, viscosity modifiers, fabric conditioning agents in solid form such as clay, fabric absorbency boosters, emulsifiers, stabilizers, shrinkage controllers, spotting agents, germicides, fungicides and anti-corrosion agents.
- The pH of the compositions of this invention is not critical, and may be anywhere in the normal range for cationic containing fabric softening compositions. The natural pH of the mixed components is ordinarily satisfactory; if adjustment is desired for any reason, trace quantities of organic or inorganic acids or bases can be used. A preferred pH range is 3.5 to 8.0; especially preferred is 4.5 to 6.5.
- The liquid fabric conditioning compositions of the present invention can be prepared by conventional methods. Homogenizing is not necessary. A convenient and satisfactory method is to prepare a premix of softeners in water at about 150°F (65.5°C) which is then added to a hot aqueous solution of the other ingredients. Temperature-sensitive optional components can be added after the fabric conditioning composition is cooled to room temperature or thereabouts.
- The liquid fabric conditioning compositions of this invention are used by adding to the rinse cycle of conventional home laundry operations. Generally, rinse water has a temperature of from about 5°C to about 60°C. The concentration of the fabric conditioners of this invention, cationic plus nonionic, is generally from about 2 ppm to about 200 ppm, preferably from about 10 ppm to about 100 ppm, by weight of the aqueous rinsing bath.
- In general, the present invention in its fabric conditioning method aspect comprises (a) washing fabrics in a conventional washing machine with a detergent composition; (b) rinsing the fabrics; (c) adding during the rinsing stage of the operation the above-described amounts of cationic and nonionic fabric conditioner in an aqueous liquid composition containing specified amounts of protonated di-polyethoxymonoalkyl amine and lower alcohol as hereinbefore defined; and (d) drying the fabrics.
- The detergent composition normally contains an anionic, nonionic, amphoteric or ampholytic surfactant or a mixture thereof, and frequently contains in addition an organic or inorganic builder. When multiple rinses are used, the fabric conditioning composition is preferably added to the final rinse. Fabric drying can take place either in the open air or in an automatic dryer.
- The following examples illustrate the aqueous liquid fabric conditioning compositions and methods of this invention and the benefits achieved by the utilization of such compositions and methods. These examples are illustrative of the invention herein and are not to be construed as limiting thereof. "Parts" stands for parts by weight.
- Example 1 was prepared by the following process:
- A softener premix was prepared as follows: 5.01 part of commercial dimethyl ditallow ammonium chloride [Adogen 448, 75.8% active, melted, 49°C] was weighed into the premix tank, followed by 2.30 parts of glycerol monostearate (melted, 65°C). Then 0.08 parts of dye solution was added [Geigy Polar Blue, 1% solution], and the premix was heated to 68°C and agitated for 3-4 minutes by an air-driven mixer.
- The ·complete composition was prepared as follows: 86.59 parts of city water [5-6 grains hardness/3.785 1) was metered into the mix tank and heated to 65°C. Then 0.0167 parts of 30% hydrogen peroxide solution was added, with agitation, followed by the addition of 1.67 parts of commercial di-polyethoxy monoalkyl amine (AMILADIN-D, 30% active, room temperature). After 1-2 minutes agitation to ensure thorough mixing, the heated softener premix prepared as described hereinbefore was added. Then 4.0 parts ethylene glycol, 0.17 parts perfume and 0.167 parts of Silicone (Dow-Corning's DC-436) were added, following which the entire composition was cooled from 65°C to 32°C with continued agitation. The pH was adjusted with dilute hydrochloric acid to 4.5. Batch size was 2000 grams.
- The material denominated above as glycol monostearate of Example 1 was prepared by esterifying hardened soybean oil with glycerine. It contained 1.4% free fatty acid, and the remainder glycerides: 37% mono, 44% di, and 19% tri. The fatty acid chains were 10.2% palmitic, 88.8% stearic and 1.0% oleic, with traces of myristic and linoleic. Iodine value was 2.0.
- Physical stability at both ambient and elevated temperature was good. It was also tested and found excellent under freeze-thaw conditions as follows: (a) in 4 cycles alternating between 24 hours at -18°C and 24 hours at 21 °C. (b) in 20 cycles alternating between 24 hours at -9.45°C and 24 hours at 21 °C; and (c) in 5 cycles alternating between 3 days at -9.45°C and 24 hours at 21 °C the compositions thickened but did not gel. For example, in condition (a) above the viscosity increased from .2 g/(cmxsec.) to .78 g/(cmxsec.).
- Example No. 1 was tested for fabric softening on cotton terry cloths and T-shirts and polyester and acrylic swatches, and was tested for antistatic effects on the foregoing synthetic fibers. It was found to be excellent in all these respects in comparison with commercially marketed products.
- Example 1 was repeated, except acid was not added to the final product and it remained at its natural pH of 5.6. Physical stability and softening performance were good; comparable in all respects to that of the product of Example 1.
- Example 2 was repeated except VARONIC T-220 was used instead of AMILADIN-D, and the batch size was increased to 400 pounds. Physical stability and softening performance were good in all respects.
- Example 1 was repeated with the variations in composition shown below:
- Physical stability and softening performance were good in all respects for each of the above compositions.
-
- Softening performance of the above compositions was good. However, after exposure to freeze-thaw cycles, the compositions were gels and no longer flowed freely.
-
- a Tallow trimethyl ammonium chloride
- b Ditallow dipropyl ammonium phosphate
- c Dicoconut diethyl ammonium chloride
- d Dihexadecyl dimethyl ammonium acetate
- e Isobutyl stearate
- f Ethylene glycol dipalmitoleate
- g Sorbitan monolaurate
- h Myristyl succinate
- i Rs has 10 carbon atoms, and (m+n)=16
- j Rs has 20 carbon atoms, and (m+n)=30
- k Rg has 14 carbon atoms, and (m+n)=10
- m R9 is derived from tallow, and (m+n)=40
- q CH3CH2OCH2CH2OH
- s CH2OHCH2OH
- t CH2OHCHOHCH3.
Claims (7)
wherein the total amount of cationic plus nonionic fabric conditioning agents is no more than 11%; and
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US45710 | 1979-06-05 | ||
US06/045,710 US4233164A (en) | 1979-06-05 | 1979-06-05 | Liquid fabric softener |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0021476A1 EP0021476A1 (en) | 1981-01-07 |
EP0021476B1 true EP0021476B1 (en) | 1983-11-30 |
Family
ID=21939452
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP80200499A Expired EP0021476B1 (en) | 1979-06-05 | 1980-05-27 | Liquid fabric softener containing a quaternary ammonium salt and method of conditioning fabrics |
Country Status (5)
Country | Link |
---|---|
US (1) | US4233164A (en) |
EP (1) | EP0021476B1 (en) |
JP (1) | JPS5626071A (en) |
CA (1) | CA1142711A (en) |
DE (1) | DE3065761D1 (en) |
Families Citing this family (46)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4320013A (en) * | 1980-06-10 | 1982-03-16 | The Procter & Gamble Company | Fabric conditioning compositions |
DE3025369A1 (en) * | 1980-07-04 | 1982-01-28 | Hoechst Ag, 6000 Frankfurt | SOFT SOFT CONDENSER CONCENTRATE |
ATE13562T1 (en) * | 1981-01-16 | 1985-06-15 | Procter & Gamble | TEXTILE TREATMENT AGENTS. |
EP0059502B1 (en) * | 1981-02-28 | 1985-06-26 | THE PROCTER & GAMBLE COMPANY | Textile treatment compositions |
DE3271812D1 (en) * | 1981-03-07 | 1986-07-31 | Procter & Gamble | Textile treatment compositions and preparation thereof |
US4464271A (en) * | 1981-08-20 | 1984-08-07 | International Flavors & Fragrances Inc. | Liquid or solid fabric softener composition comprising microencapsulated fragrance suspension and process for preparing same |
US4446032A (en) * | 1981-08-20 | 1984-05-01 | International Flavors & Fragrances Inc. | Liquid or solid fabric softener composition comprising microencapsulated fragrance suspension and process for preparing same |
US4454049A (en) * | 1981-11-14 | 1984-06-12 | The Procter & Gamble Company | Textile treatment compositions |
DE3204165A1 (en) * | 1982-02-06 | 1983-08-11 | Hoechst Ag, 6230 Frankfurt | CONCENTRATED SOFT SOFTENER |
GB2115847B (en) * | 1982-03-02 | 1984-04-04 | Derek James Frost | Antistatic composition for synthetic textile materials |
DE3218667A1 (en) * | 1982-05-18 | 1983-11-24 | Hoechst Ag, 6230 Frankfurt | CONCENTRATED SOFT SOFTENER |
EP0116512A1 (en) * | 1983-02-10 | 1984-08-22 | Sherex Chemical Company, Inc. | Fiber debonder formulation comprising diamido quaternary ammonium compound and alkoxylated fatty acid |
US4497718A (en) * | 1983-04-20 | 1985-02-05 | Lever Brothers Company | Homogeneous aqueous fabric softening composition with stilbene sulfonic acid fluorescent whitener |
US4562002A (en) * | 1983-04-20 | 1985-12-31 | Lever Brothers Company | Homogeneous aqueous fabric softening composition with stilbene sulfonic acid fluorescent whitener |
US4661270A (en) * | 1983-05-11 | 1987-04-28 | Colgate-Palmolive Company | Concentrated fabric softening composition and methods for making same |
NZ207932A (en) * | 1983-05-11 | 1986-03-14 | Colgate Palmolive Co | Fabric softener compositions containing quaternary ammonium compounds |
EP0128231B1 (en) * | 1983-06-10 | 1987-09-09 | S.A. Camp Fábrica de Jabones | Stable concentrated aqueous dispersions of water-insoluble cationic compounds and preparation thereof |
JPS6072831A (en) * | 1983-09-29 | 1985-04-24 | Kao Corp | Composition for vesicle |
FR2564495B1 (en) * | 1984-05-16 | 1987-02-27 | Stepan Europe | CONCENTRATED SOFTENING COMPOSITIONS BASED ON CATIONIC QUATERNARY AMMONIUM SURFACTANTS |
DE3500877A1 (en) * | 1985-01-12 | 1986-07-17 | Henkel KGaA, 4000 Düsseldorf | HAIR DYE PREPARATION |
US4698259A (en) * | 1985-08-21 | 1987-10-06 | Hervey Laurence R B | Use of oxonated poly(alkylene oxides) as surface treatment agents |
US4643919A (en) * | 1986-02-06 | 1987-02-17 | The Procter & Gamble Company | Textile treating compositions and methods |
US4767548A (en) * | 1986-08-06 | 1988-08-30 | Dow Corning Corporation | Articles for conditioning fabrics in a laundry dryer |
JP2522659B2 (en) * | 1987-03-31 | 1996-08-07 | ライオン株式会社 | Softener composition |
GB8722540D0 (en) * | 1987-09-24 | 1987-10-28 | Unilever Plc | Composition for softening fabrics |
DE3823843A1 (en) * | 1988-07-14 | 1990-01-18 | Henkel Kgaa | HAIR DYE PREPARATION |
GB8916308D0 (en) * | 1989-07-17 | 1989-08-31 | Unilever Plc | Fabric softening |
WO1993019156A1 (en) * | 1992-03-16 | 1993-09-30 | The Procter & Gamble Company | Process for preparing concentrated imidazoline fabric softener compositions |
US5827451A (en) * | 1993-03-17 | 1998-10-27 | Witco Corporation | Microemulsion useful as rinse aid |
US5616553A (en) * | 1993-08-12 | 1997-04-01 | The Procter & Gamble Company | Fabric conditioning compositions |
US5599786A (en) * | 1993-08-12 | 1997-02-04 | The Procter & Gamble Company | Cellulase fabric-conditioning compositions |
AU2399295A (en) * | 1994-04-29 | 1995-11-29 | Procter & Gamble Company, The | Cellulase fabric-conditioning compositions |
DE4420188A1 (en) * | 1994-06-09 | 1995-12-14 | Hoechst Ag | Fabric softener concentrates |
US5445747A (en) * | 1994-08-05 | 1995-08-29 | The Procter & Gamble Company | Cellulase fabric-conditioning compositions |
DE69534903T2 (en) | 1995-08-31 | 2007-01-18 | The Procter & Gamble Company, Cincinnati | Use of allyl alcohol as a bad odor reducing agent |
ATE235544T1 (en) | 1996-10-30 | 2003-04-15 | Procter & Gamble | FABRIC PLASTICIZER COMPOSITIONS |
EP0890671A3 (en) * | 1997-07-10 | 2000-02-23 | Ciba SC Holding AG | Use of modified fatty amines for preventing deposition of low molecular weight by-products on textile materials |
US6818610B2 (en) * | 2001-07-27 | 2004-11-16 | Procter & Gamble Company | Fabric care systems for providing anti-wrinkle benefits to fabric |
US7901699B2 (en) * | 2004-06-30 | 2011-03-08 | The Nisshin Oillio Group, Ltd. | Cosmetic composition and cosmetics |
US7405187B2 (en) | 2006-06-01 | 2008-07-29 | The Procter & Gamble Company | Concentrated perfume compositions |
US7304027B1 (en) | 2006-07-31 | 2007-12-04 | The Dial Corporation | Phase-stable concentrated fabric softeners containing borates |
DE102007012910A1 (en) | 2007-03-19 | 2008-09-25 | Momentive Performance Materials Gmbh | Fragrance-modified, branched polyorganosiloxanes |
DE102007012909A1 (en) | 2007-03-19 | 2008-09-25 | Momentive Performance Materials Gmbh | Fragrance-modified, reactive polyorganosiloxanes |
WO2015164677A1 (en) | 2014-04-23 | 2015-10-29 | Gregory Van Buskirk | Cleaning formulations for chemically sensitive individuals: compositions and methods |
AU2016206650A1 (en) | 2015-01-14 | 2017-08-10 | Gregory Van Buskirk | Improved fabric treatment method for stain release |
US11441106B2 (en) | 2017-06-27 | 2022-09-13 | Henkel Ag & Co. Kgaa | Particulate fragrance enhancers |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB947714A (en) * | 1960-07-18 | 1964-01-29 | Armour Chemical Ind Ltd | Improvements in or relating to surface active compositions |
DE2025945A1 (en) * | 1970-05-27 | 1971-12-16 | Henkel & Cie GmbH, 4000 Düsseldorf | Liquid fabric softener |
US3952128A (en) * | 1971-09-01 | 1976-04-20 | Kao Soap Co., Ltd. | Durable antistatic agent, hydrophobic fibers and fibrous structures having durable antistatic property and method of making same |
US3954634A (en) * | 1973-07-27 | 1976-05-04 | S. C. Johnson & Son, Inc. | Stable, low-viscosity fabric softener |
US3958059A (en) * | 1973-10-01 | 1976-05-18 | The Procter & Gamble Company | Fabric treatment composition |
US4022938A (en) * | 1974-04-16 | 1977-05-10 | The Procter & Gamble Company | Fabric treatment compositions |
US4045361A (en) * | 1975-05-21 | 1977-08-30 | The Procter & Gamble Company | Fabric conditioning compositions |
LU75088A1 (en) * | 1976-06-04 | 1978-01-18 | ||
US4076632A (en) * | 1977-02-22 | 1978-02-28 | The Procter & Gamble Company | Fabric softener |
US4155855A (en) * | 1977-07-06 | 1979-05-22 | The Procter & Gamble Company | Concentrated liquid fabric softener composition |
US4157307A (en) * | 1978-08-07 | 1979-06-05 | The Procter & Gamble Company | Liquid fabric softener |
-
1979
- 1979-06-05 US US06/045,710 patent/US4233164A/en not_active Expired - Lifetime
-
1980
- 1980-05-27 DE DE8080200499T patent/DE3065761D1/en not_active Expired
- 1980-05-27 EP EP80200499A patent/EP0021476B1/en not_active Expired
- 1980-06-04 CA CA000353388A patent/CA1142711A/en not_active Expired
- 1980-06-05 JP JP7604080A patent/JPS5626071A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
US4233164A (en) | 1980-11-11 |
JPS6245352B2 (en) | 1987-09-25 |
DE3065761D1 (en) | 1984-01-05 |
EP0021476A1 (en) | 1981-01-07 |
JPS5626071A (en) | 1981-03-13 |
CA1142711A (en) | 1983-03-15 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP0021476B1 (en) | Liquid fabric softener containing a quaternary ammonium salt and method of conditioning fabrics | |
US4157307A (en) | Liquid fabric softener | |
US4126562A (en) | Textile treatment compositions | |
US4162984A (en) | Textile treatment compositions | |
EP0060003B1 (en) | Textile treatment compositions and preparation thereof | |
US4128484A (en) | Fabric softening compositions | |
EP0002085B1 (en) | Textile conditioning compositions with low content of cationic guar gum | |
USRE34062E (en) | Fabric softening composition contains water-insoluble surfactant and aliphatic mono-carboxylic acid | |
US4149978A (en) | Textile treatment composition | |
CA1179806A (en) | Fabric softener concentrate | |
US4555349A (en) | Fabric softening compositions | |
KR950003851B1 (en) | Mono-ester as fiber and fabric treatment composition | |
US4844823A (en) | Fabric softener composition containing di-esterified long chain fatty acid quaternary ammonium salt | |
US4045361A (en) | Fabric conditioning compositions | |
US4076632A (en) | Fabric softener | |
EP0059502B1 (en) | Textile treatment compositions | |
EP0787793B1 (en) | Fabric softening composition | |
JPS61179372A (en) | Cloth softening composition | |
US4320013A (en) | Fabric conditioning compositions | |
CA1329682C (en) | Isotropic fabric softener composition containing fabric mildewstat | |
EP0288137A2 (en) | Method of conditioning fabrics | |
GB1601359A (en) | Textile treating composition | |
JPH08505905A (en) | Textile product softening composition | |
CA1152707A (en) | Fabric softener | |
JPH07268773A (en) | Soft finishing agent composition for textile good and its preparation |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
AK | Designated contracting states |
Designated state(s): BE DE FR GB IT NL |
|
17P | Request for examination filed |
Effective date: 19810626 |
|
ITF | It: translation for a ep patent filed | ||
GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
AK | Designated contracting states |
Designated state(s): BE DE FR GB IT NL |
|
REF | Corresponds to: |
Ref document number: 3065761 Country of ref document: DE Date of ref document: 19840105 |
|
ET | Fr: translation filed | ||
PLBE | No opposition filed within time limit |
Free format text: ORIGINAL CODE: 0009261 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT |
|
26N | No opposition filed | ||
ITTA | It: last paid annual fee | ||
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: FR Payment date: 19940511 Year of fee payment: 15 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: GB Payment date: 19940517 Year of fee payment: 15 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DE Payment date: 19940524 Year of fee payment: 15 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: NL Payment date: 19940531 Year of fee payment: 15 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: BE Payment date: 19940711 Year of fee payment: 15 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: GB Effective date: 19950527 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: BE Effective date: 19950531 |
|
BERE | Be: lapsed |
Owner name: THE PROCTER & GAMBLE CY Effective date: 19950531 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: NL Effective date: 19951201 |
|
GBPC | Gb: european patent ceased through non-payment of renewal fee |
Effective date: 19950527 |
|
NLV4 | Nl: lapsed or anulled due to non-payment of the annual fee |
Effective date: 19951201 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: DE Effective date: 19960201 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: FR Effective date: 19960229 |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: ST |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: ST |